Derivatives of benzo[h]naphtho[1,2-f]quinoline and organic light emitting devices (OLEDs) including them are disclosed. The subject compounds impart high efficiency, low driving voltage, high luminance and long lifespan to the OLEDs. The subject compounds may be used as light emitting materials, as electron transporting materials, or as electron injecting materials. Because the subject compounds have high glass transition temperatures or high melting points, OLEDs including them exhibit high durability in storage or operation. Suitable substituents may be selected from deuterium, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, aryloxy, arylthio, aryl, aryl- or heteroaryl-substituted amino, heteroaryl, condensed polycyclic, halogen, cyano, nitro, hydroxyl and carboxyl groups.

Claims

19 · 1 independent · depth 5

19 granted claims

›1.independentA heterocyclic compound represented by Formula 1 below:+18

›2.↳ 1The heterocyclic compound of claim 1, wherein R1, R2, and R8 in Formula 1 are each independently a substituted or unsubstituted C6-C20 aryl group, a s…d2

›3.↳ 1The heterocyclic compound of claim 1, wherein R3 to R7, and R9 to R13 in Formula 1 are each independently a hydrogen atom or a deuterium atom.d2

›4.↳ 1The heterocyclic compound of claim 1, R1 and R2 in Formula 1 each being independently selected from the group consisting of a hydrogen atom, a deuteri…d2

›5.↳ 1The heterocyclic compound of claim 1, R8 in Formula 1 being one of the groups represented by Formulae 3a to 3j below:d2

›6.↳ 1The heterocyclic compound of claim 1, R1 and R2 in Formula 1 each being independently selected from the group consisting of a hydrogen atom, a deuteri…d2

›7.↳ 1The heterocyclic compound of claim 1, R8 in Formula 1 being one of the groups represented by Formulae 5a to 5o below:d2

›8.↳ 1The heterocyclic compound of claim 1, the compound of Formula 1 comprising one of the compounds below:d2

›9.↳ 1An organic light-emitting device comprising:na first electrode;a second electrode; andan organic layer between the first electrode and the second elec…d2+9

›10.↳ 9The organic light-emitting device of claim 9, wherein the first layer comprises at least one layer selected from the group consisting of a hole inject…d3

›11.↳ 9The organic light-emitting device of claim 9, wherein the first layer comprises at least one layer selected from the group consisting of a hole inject…d3

›12.↳ 9The organic light-emitting device of claim 9, wherein the organic layer further comprises a hole injection layer, a hole transport layer, a functional…d3+5

›19.↳ 9A flat panel display device comprising the organic light-emitting device of claim 9, wherein the first electrode of the organic light-emitting device …d3

›18.↳ 1multiple · 1, 9The organic light-emitting device of claim 9, wherein the first layer comprising the heterocyclic compound of Formula 1 of claim 1 is formed using a w…d2

Classifications

14 codes

IPC · International Patent Classification

Section C — Chemistry; metallurgy

C07D401/10
C09K11/06
C07D401/14
C07D401/12
C07D221/18

Section H — Electricity

H01L51/00
H01L51/54
H01L51/50

USPC · US Patent Classification

428/690546/42257/40544/180257/E51.024428/917

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3.0 y

1,091 days filing → grant

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non-final + final

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no RCE

Examiner

Andrew K Bohaty

art unit 1786 · TC 1700

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1 priority documents

›Priority documents — 1

Type	Document	Date
related publication	US 20130001529 A1	3 Jan 2013

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